Study to Compare Efficacy of Topical ARYS-01 (Sorivudine) Cream 3%, Oral Valaciclovir and Combination ARYS-01 Cream 3%/Oral Valaciclovir for Treatment of Herpes Zoster (Shingles)
Primary Purpose
Herpes Zoster, Postherpetic Neuralgia
Status
Unknown status
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
ARYS-01 (sorivudine) cream 3% or placebo cream
placebo
valaciclovir
Sponsored by
About this trial
This is an interventional treatment trial for Herpes Zoster focused on measuring antiviral, herpes zoster, postherpetic neuralgia, varicella zoster virus, shingles
Eligibility Criteria
Inclusion Criteria:
- at least 18 years of age
- diagnosed with herpes zoster
- confirmed for VZV with lesion swab at screening and subsequent PCR test.
- contraception for women of child-bearing potential
- be able to communicate with investigator and compliant
Exclusion Criteria:
- cytotoxic or immunosuppressive drugs within 3 mos, 5-FU or its pro-drugs, tricyclic antidepressants, probenecid, topical or systemic antiviral drugs or immunomodulatory agents for viral infection
- herpes zoster ophthalmicus
- female patients who are pregnant and/or nursing or planning a pregnancy
- congenital, acquired or corticosteroid-induced immunodeficiency, including malignancy
- renal insufficiency or creatinine level >2mg/dL
- clinical significant liver enzyme abnormalities and any other laboratory abnormalities determined by the screening lab
- history of intolerance or hypersensitivity to the cream components
- current significant skin disease within affected dermatome
- history of positive result for hepatitis B surface antigen, hepatitis C virus, or HIV
- current participation in another clinical drug research study
Sites / Locations
- ARYS-0701 Site 3
- ARYS-0701 Site 6
- ARYS-0701 Site 7
- ARYS-0701 Site 8
- ARYS-0701 Site 9
- ARYS-0701 Site 10
- ARYS-0701 Site 11
- ARYS-0701 Site 4
- ARYS-0701 Site 12
- ARYS-0701 Site 1
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Placebo Comparator
Active Comparator
Experimental
Other
Arm Label
1
2
3
4
Arm Description
Placebo cream BID for 10 days and placebo valaciclovir caplets TID from days 1-3 and active valaciclovir caplets 1 gram TID from days 4-10
Placebo cream BID for 10 days and active valaciclovir caplets TID from days 1-10
Active cream BID for 10 days and placebo valaciclovir caplets TID from days 1-3 and active valaciclovir caplets 1 gram TID from days 4-10
Active cream BID for 10 days and active valaciclovir caplets TID from days 1-10
Outcomes
Primary Outcome Measures
The effect of ARYS-01 (sorivudine) cream (with or without Valaciclovir) on the reduction of the crusting stage of VZV rash present at Day 8.
Secondary Outcome Measures
The time to cessation of new lesion formation, and time to cessation of Zoster-associated pains, pain intensity, rash healing and size reduction, and lesion dissemination.
Full Information
NCT ID
NCT00652184
First Posted
April 1, 2008
Last Updated
October 3, 2008
Sponsor
aRigen Pharmaceuticals, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT00652184
Brief Title
Study to Compare Efficacy of Topical ARYS-01 (Sorivudine) Cream 3%, Oral Valaciclovir and Combination ARYS-01 Cream 3%/Oral Valaciclovir for Treatment of Herpes Zoster (Shingles)
Official Title
Phase 2/3 Multi-Center, Double-Blind, Controlled Trial Comparing Topical ARYS-01 (Sorivudine) Cream 3%, Oral Valaciclovir, and Combination Topical ARYS-01 Cream /Oral Valaciclovir for Treatment of Herpes Zoster in Immunocompetent Patients 18 Years of Age or Older
Study Type
Interventional
2. Study Status
Record Verification Date
October 2008
Overall Recruitment Status
Unknown status
Study Start Date
March 2008 (undefined)
Primary Completion Date
June 2009 (Anticipated)
Study Completion Date
September 2009 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
aRigen Pharmaceuticals, Inc.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
A multi-center, randomized, 4-arm, placebo-controlled, double-blind efficacy study of ARYS-01 (sorivudine) cream 3%.
Detailed Description
More than 95% of people are infected with varicella Zoster virus (VZV) at one time of life or another. Primary VZV infection manifests as varicella (chicken pox). The virus then establishes a latent infection of the sensory ganglia from which it may reactivate years later to produce the clinical syndrome of Herpes Zoster (shingles). The initial cutaneous VZV lesions are pruritic, erythematous macules; and the lesions progress through maculopapular stage to vesicular, ulceration and crusting phases. The crusting phase signals the beginning of the healing process, and begins with clouding of the vesicular fluid, within about 24 to 48 h after the appearance of each lesion. This is a Phase 2 study to assess: 1) the overall benefit of ARYS-01 (sorivudine) cream 3% vs. Placebo cream (with immediate or delayed use of Valaciclovir therapy) on Herpes Zoster rash healing rates and postherpetic neuralgia (PHN), 2) the efficacy of ARYS-01 cream 3% vs. Placebo cream, prior to initiation of Valaciclovir, to build evidence for monotherapy treatment benefit of ARYS-01 cream on the initial onset of Herpes Zoster symptoms, 3) the efficacy of ARYS-01 cream 3% vs. Placebo cream, with immediate or delayed initiation of Valaciclovir, for synergetic effects on the initial onset of Herpes Zoster symptoms.
The primary efficacy endpoint is the effect of ARYS-01 cream (with or without Valaciclovir) on the reduction of the crusting stage of VZV rash present at Day 8. Secondary endpoints include time to cessation of new lesion formation, and time to cessation of Zoster-associated pains, pain intensity, rash healing and size reduction, and lesion dissemination.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Herpes Zoster, Postherpetic Neuralgia
Keywords
antiviral, herpes zoster, postherpetic neuralgia, varicella zoster virus, shingles
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
300 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Placebo Comparator
Arm Description
Placebo cream BID for 10 days and placebo valaciclovir caplets TID from days 1-3 and active valaciclovir caplets 1 gram TID from days 4-10
Arm Title
2
Arm Type
Active Comparator
Arm Description
Placebo cream BID for 10 days and active valaciclovir caplets TID from days 1-10
Arm Title
3
Arm Type
Experimental
Arm Description
Active cream BID for 10 days and placebo valaciclovir caplets TID from days 1-3 and active valaciclovir caplets 1 gram TID from days 4-10
Arm Title
4
Arm Type
Other
Arm Description
Active cream BID for 10 days and active valaciclovir caplets TID from days 1-10
Intervention Type
Drug
Intervention Name(s)
ARYS-01 (sorivudine) cream 3% or placebo cream
Other Intervention Name(s)
ARYS-01 cream 3%, sorivudine cream 3%, topical sorivudine 3%
Intervention Description
sorivudine cream 3% or placebo cream twice daily for 10 days
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
placebo cream and placebo valaciclovir
Intervention Type
Drug
Intervention Name(s)
valaciclovir
Intervention Description
active valaciclovir
Primary Outcome Measure Information:
Title
The effect of ARYS-01 (sorivudine) cream (with or without Valaciclovir) on the reduction of the crusting stage of VZV rash present at Day 8.
Time Frame
Day 8
Secondary Outcome Measure Information:
Title
The time to cessation of new lesion formation, and time to cessation of Zoster-associated pains, pain intensity, rash healing and size reduction, and lesion dissemination.
Time Frame
Day 4
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
at least 18 years of age
diagnosed with herpes zoster
confirmed for VZV with lesion swab at screening and subsequent PCR test.
contraception for women of child-bearing potential
be able to communicate with investigator and compliant
Exclusion Criteria:
cytotoxic or immunosuppressive drugs within 3 mos, 5-FU or its pro-drugs, tricyclic antidepressants, probenecid, topical or systemic antiviral drugs or immunomodulatory agents for viral infection
herpes zoster ophthalmicus
female patients who are pregnant and/or nursing or planning a pregnancy
congenital, acquired or corticosteroid-induced immunodeficiency, including malignancy
renal insufficiency or creatinine level >2mg/dL
clinical significant liver enzyme abnormalities and any other laboratory abnormalities determined by the screening lab
history of intolerance or hypersensitivity to the cream components
current significant skin disease within affected dermatome
history of positive result for hepatitis B surface antigen, hepatitis C virus, or HIV
current participation in another clinical drug research study
Facility Information:
Facility Name
ARYS-0701 Site 3
City
Beverly Hills
State/Province
California
ZIP/Postal Code
90211
Country
United States
Facility Name
ARYS-0701 Site 6
City
Encino
State/Province
California
ZIP/Postal Code
91436
Country
United States
Facility Name
ARYS-0701 Site 7
City
Vista
State/Province
California
ZIP/Postal Code
92083
Country
United States
Facility Name
ARYS-0701 Site 8
City
Henderson
State/Province
Nevada
ZIP/Postal Code
89014
Country
United States
Facility Name
ARYS-0701 Site 9
City
Las Vegas
State/Province
Nevada
ZIP/Postal Code
89106
Country
United States
Facility Name
ARYS-0701 Site 10
City
New York
State/Province
New York
ZIP/Postal Code
10003
Country
United States
Facility Name
ARYS-0701 Site 11
City
New York
State/Province
New York
ZIP/Postal Code
10029
Country
United States
Facility Name
ARYS-0701 Site 4
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Facility Name
ARYS-0701 Site 12
City
Raleigh
State/Province
North Carolina
ZIP/Postal Code
27612
Country
United States
Facility Name
ARYS-0701 Site 1
City
Houston
State/Province
Texas
ZIP/Postal Code
77058
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
19469706
Citation
Satyaprakash AK, Tremaine AM, Stelter AA, Creed R, Ravanfar P, Mendoza N, Mehta SK, Rady PL, Pierson DL, Tyring SK. Viremia in acute herpes zoster. J Infect Dis. 2009 Jul 1;200(1):26-32. doi: 10.1086/599381.
Results Reference
derived
Learn more about this trial
Study to Compare Efficacy of Topical ARYS-01 (Sorivudine) Cream 3%, Oral Valaciclovir and Combination ARYS-01 Cream 3%/Oral Valaciclovir for Treatment of Herpes Zoster (Shingles)
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